反应条件
1.1: boron trifluoride diethyl etherate / dichloromethane / 2 h / 0 - 20 °C 2.1: sodium methylate / methanol / 20 °C 3.1: toluene-4-sulfonic acid / N,N-dimethyl-formamide / 20 °C 4.1: sodium hydride / N,N-dimethyl-formamide / 0.75 h / 0 °C 4.2: 3 h 5.1: trifluoroacetic acid / dichloromethane; water / 24 h / 20 °C 6.1: 2-aminoethyl diphenylborinate; N-ethyl-N,N-diisopropylamine / acetonitrile / 22 h / 20 °C 7.1: lithium aluminium tetrahydride / tetrahydrofuran; diethyl ether / 1 h / 0 °C / |Reflux 8.1: ReOCl3(SMe2)(OPPh3) / benzene / 72 h / 0 °C 9.1: tetrabutyl ammonium fluoride / tetrahydrofuran 10.1: ReOCl3(SMe2)(OPPh3) / benzene / 60 h / 0 °C 11.1: LiDBB / tetrahydrofuran / 0.25 h / -20 °C 12.1: 1H-imidazole / N,N-dimethyl-formamide / 40 h / 20 - 50 °C 13.1: triphenylphosphine hydrobromide / chloroform / 24 h / 20 °C / |Molecular sieve 14.1: ammonium fluoride-hydrogen fluoride / N,N-dimethyl-formamide; 1-methyl-pyrrolidin-2-one / 144 h / 80 °C View Scheme
参考文献
Journal of Organic Chemistry, , vol. 78, # 24 p. 12469 - 12476